Posterior Fixation

Posterior semi-rigid osteosynthesis system VEOS PEEK-OPTIMA™ Image Contrast

Semi-rigid posterior osteosynthesis system

VEOS PEEK-OPTIMA™ Image Contrast is a top loading posterior fixation system offering the possibility to perform semi-rigid posterior fixation.

VEOS is part the the VEOS-KAPHORN modular platform of implants and instruments, offering an innovative and versatile solution to adapt to surgeon's needs: several specific implants and instruments modules are organized around a universal base.

Easy to use and fully modular, the platform simplify equipment management while giving the surgeons a wide range of possibility in terms of technologies, surgical approaches and treament solutions.

Informations

VEOS is a top loading posterior fixation system offering the possibility to perform semi-rigid posterior fixation with PEEK-OPTIMA™ rods.

VEOS implants are available in a range of shapes and sizes for screws, locking screws, rods and connectors.

Implants material
• PEEK OPTIMA LT1-6BA (norme ASTM F2026).

Instruments material
• Stainless steel (EN 10088-2, EN 10216-5, ASTM A213), titanium (5832-3 or 5832-2), polymers

Indications
VEOS system can be used in skeletally mature individuals (adults) for the posterior fixation of the lumbar spine.

It is indicated for the treatment of the degenerative spine.

VEOS can also be used in revision surgery in case of failure of a previous procedure.

Features

  • 2 screw options: solid and cannulated-fenestrated
  • Polyaxial, monoaxial and polyaxial reduction screws
  • Double threaded solid screw
  • Quadruple and double threaded cannulated screw
  • PEEK rods: to perform semi-rigid constructs and help reduce the risk of adjacent segment syndrom
  • Barium sulfate integrated into PEEK to facilitate imaging controls

Product Range

  • 5 screw diameters (ø4.5 to 8.5 mm) of polyaxial, monoaxial and reduction screws
  • Pre-bent PEEK-OPTIMA™ rods, 5.5 mm diameter. Length: 40 to 130 mm

Regulatory Notices

VEOS system can be used in skeletally mature individuals (adults) and in adolescent population for specific indications such as scoliosis.

This medical device is intended for the posterior fixation of the thoracic, lumbar and sacral spine. It is indicated for the treatment of deformities (any etiology), trauma, tumors, and the degenerative spine (spondylolisthesis, degenerative disc disease, spinal fractures, spinal stenosis, non-union). VEOS can also be used in revision surgery in case of failure of a previous procedure.

Please read the informations in the instructions for use carefully.

VEOS implants are class IIb healthcare products marked CE2803 under the relevant European regulations.
For proper implantation, VEOS must be used with a specific set of Class I instruments and reusable surgical instruments marked CE/CE0197 under the appropriate European regulations.

The use of these instruments is described in the surgical technique.

Manufacturer 
DISTIMP: 7, allée du Moulin Berger 69130 Ecully, France

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